Gene: CSRNP2
Official Full Name: cysteine and serine rich nuclear protein 2provided by HGNC
Gene Summary: The protein encoded by this gene belongs to the CSRNP family of nuclear proteins that share conserved regions, including cysteine- and serine- rich regions, a basic domain, a transcriptional activation domain, and bind the sequence 'AGAGTG', thus have the hallmark of transcription factors. Studies in mice suggest that these genes may have redundant functions. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO25742 | CSRNP2 Knockout cell line (HeLa) | Human | CSRNP2 | 1:3~1:6 | Negative | Online Inquiry |
KO25743 | CSRNP2 Knockout cell line (HCT 116) | Human | CSRNP2 | 1:2~1:4 | Negative | Online Inquiry |
KO25744 | CSRNP2 Knockout cell line (HEK293) | Human | CSRNP2 | 1:3~1:6 | Negative | Online Inquiry |
KO25745 | CSRNP2 Knockout cell line (A549) | Human | CSRNP2 | 1:3~1:4 | Negative | Online Inquiry |
CSRNP2 Gene Knockout Cell Lines are genetically modified cell lines in which the CSRNP2 gene has been disrupted, allowing researchers to investigate the biological roles and pathways involving this gene. CSRNP2, or cysteine and serine-rich nuclear protein 2, is implicated in various cellular processes, including transcriptional regulation and cellular stress responses. By utilizing CSRNP2 knockout cell lines, scientists can elucidate the functional significance of this gene in diverse contexts, enhancing our understanding of gene function and gene-environment interactions.
The primary mechanism of action for these cell lines involves the use of CRISPR/Cas9 technology or similar gene-editing tools to create targeted disruptions in the CSRNP2 gene. This precise approach permits researchers to generate isogenic lines that are otherwise identical at the genetic level, aside from the knockout of CSRNP2. Such controlled experiments allow for robust comparative studies, making it easier to ascertain the gene's impact on cellular behavior, signaling pathways, and response to pharmacological agents.
The scientific importance of CSRNP2 knockout cell lines is substantiated by their utility in various fields, including cancer research, neurobiology, and pharmacogenomics. In clinical settings, understanding the function of the CSRNP2 gene can reveal its relevance to disease mechanisms, potentially leading to the identification of novel therapeutic targets or biomarkers.
What sets CSRNP2 Gene Knockout Cell Lines apart from alternatives is their high specificity and reproducibility. Unlike traditional knockout methods that can produce off-target effects and variability, our expertly developed cell lines ensure that the targeted mutation is precise, yielding consistent results across experiments. This reliability enhances the credibility of scientific findings, making them more likely to withstand scrutiny in the peer-review process.
Ultimately, the value of CSRNP2 Gene Knockout Cell Lines lies in their ability to facilitate groundbreaking research that can translate into clinical advancements. By providing a reliable platform for gene function studies, these cell lines empower researchers and clinicians to delve deeper into the complexities of gene interactions, ultimately fostering progress in understanding and treating diseases.
Our company possesses extensive experience in developing high-quality biological products tailored to the needs of researchers and healthcare professionals. With a dedication to innovation and excellence, our offerings are designed to support pivotal discoveries in the life sciences, ensuring that our clients have the tools necessary for impactful research.
Please note that all services are for research use only. Not intended for any clinical use.
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